Canonical Allele Identifier: CA2667539849
Gene: GATA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.128480623_128480624insTA , CM000665.2:g.128480623_128480624insTA GRCh38
NC_000003.11:g.128199466_128199467insTA , CM000665.1:g.128199466_128199467insTA GRCh37
NC_000003.10:g.129682156_129682157insTA NCBI36
NG_029334.1:g.17564_17565insTA , LRG_295:g.17564_17565insTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000487848.6:c.*395_*396insTA MANE Plus Clinical ENSP00000417074.1:n.*395_*396insTA
ENST00000696466.1:c.*395_*396insTA ENSP00000512647.1:n.*395_*396insTA
ENST00000696672.1:c.813_814insTA ENSP00000512796.1:n.813_814insTA
ENST00000341105.7:c.*395_*396insTA MANE Select ENSP00000345681.2:n.*395_*396insTA
ENST00000341105.6:c.*395_*396insTA ENSP00000345681.2:n.*395_*396insTA
ENST00000430265.6:c.*395_*396insTA ENSP00000400259.2:n.*395_*396insTA
ENST00000489987.1:n.955_956insTA
NM_001145661.1:c.*395_*396insTA , LRG_295t1:c.*395_*396insTA NP_001139133.1:n.*395_*396insTA
NM_001145662.1:c.*395_*396insTA NP_001139134.1:n.*395_*396insTA
NM_032638.4:c.*395_*396insTA , LRG_295t2:c.*395_*396insTA NP_116027.2:n.*395_*396insTA
NM_001145661.2:c.*395_*396insTA MANE Plus Clinical NP_001139133.1:n.*395_*396insTA
NM_032638.5:c.*395_*396insTA MANE Select NP_116027.2:n.*395_*396insTA